Canonical Allele Identifier: PA096296
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16135
ClinVar RCV Id: RCV000426797 RCV001507008 RCV003325940 RCV003445078 RCV000017515
ClinVar Variation Id: 447418
ClinVar RCV Id: RCV000517324 RCV003325963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly261Arg
CA126211
NM_000162.5:c.781G>A
CA367400571
NM_000162.5:c.781G>C